Abstract: Described are a solid material which has ionic conductivity for lithium ions, a process for preparing said solid material, a use of said solid material as a solid electrolyte for an electrochemical cell, a solid structure selected from the group consisting of a cathode, an anode and a separator for an electrochemical cell comprising the solid material, and an electrochemical cell comprising such solid structure.

Abstract: Disclosed herein is a process for making a coated cathode active material, where the process includes the following steps: (a) providing an electrode active material according to general formula Li1+xTM1?xO2, where TM is a combination of metals according to general formula (I), and x is in the range of from zero to 0.2, with a moisture content in the range of from 500 to 1,500 ppm, (b) reacting the electrode active material with a silicon alkoxide and an alkyl aluminum compound in one or more sub-steps, and (c) heat-treating the material so obtained in an oxygen-containing atmosphere at a temperature in the range of from 100 to 400° C. for 10 minutes to 4 hours.

Abstract: Described are a coated particulate material for use in an electrode of an electrochemical cell and a process for preparing said coated particulate material, an electrode comprising said coated particulate material for use in an electrochemical cell, an electrochemical cell comprising said coated particulate material, and a use of said coated particulate material for preparing an electrode for use in an electrochemical cell.

Abstract: A mesoporous, nanocrystalline, metal oxide construct particularly suited for capacitive energy storage that has an architecture with short diffusion path lengths and large surface areas and a method for production are provided. Energy density is substantially increased without compromising the capacitive charge storage kinetics and electrode demonstrates long term cycling stability. Charge storage devices with electrodes using the construct can use three different charge storage mechanisms immersed in an electrolyte: (1) cations can be stored in a thin double layer at the electrode/electrolyte interface (non-faradaic mechanism); (2) cations can interact with the bulk of an electroactive material which then undergoes a redox reaction or phase change, as in conventional batteries (faradaic mechanism); or (3) cations can electrochemically adsorb onto the surface of a material through charge transfer processes (faradaic mechanism).

Abstract: Disclosed herein is a process for making a coated cathode active material, where the process includes the following steps: (a) providing an electrode active material according to general formula Li1+xTM1?xO2, where TM is a combination of metals according to general formula (I), and x is in the range of from zero to 0.2, with a moisture content in the range of from 500 to 1,500 ppm, (b) reacting the electrode active material with a silicon alkoxide and an alkyl aluminum compound in one or more sub-steps, and (c) heat-treating the material so obtained in an oxygen-containing atmosphere at a temperature in the range of from 100 to 400° C. for 10 minutes to 4 hours.

Abstract: A mesoporous, nanocrystalline, metal oxide construct particularly suited for capacitive energy storage that has an architecture with short diffusion path lengths and large surface areas and a method for production are provided. Energy density is substantially increased without compromising the capacitive charge storage kinetics and electrode demonstrates long term cycling stability. Charge storage devices with electrodes using the construct can use three different charge storage mechanisms immersed in an electrolyte: (1) cations can be stored in a thin double layer at the electrode/electrolyte interface (non-faradaic mechanism); (2) cations can interact with the bulk of an electroactive material which then undergoes a redox reaction or phase change, as in conventional batteries (faradaic mechanism); or (3) cations can electrochemically adsorb onto the surface of a material through charge transfer processes (faradaic mechanism).

Abstract: Process for making a particulate lithiated transition metal oxide comprising the steps of: (a) Providing a particulate transition metal precursor comprising Ni, (b) mixing said precursor with at least one compound of lithium and at least one processing additive selected from NaCl, KCl, CuCl2, B2O3, MoO3, Bi2O3, Na2SO4, and K2SO4 in an amount of from 0.1 to 5% by weight, referring to the entire mixture obtained in step (b), (c) thermally treating the mixture obtained according to step (b) in at least two steps, (c1) at 300 to 500° C. under an atmosphere that may comprise oxygen, (c2) at 650 to 850° C. under an atmosphere of oxygen.

Abstract: Process for making a lithiated oxide, said process comprising the following steps: (a) making a particulate hydroxide, oxide or oxyhydroxide of nickel, and, optionally, at least one of Co and Mn and, by combining an aqueous solution of sodium or potassium hydrox-ide with an aqueous solution containing a water-soluble salt of nickel and, optionally, a water-soluble salt of Co, Mn, Al, Ti, Zr, W, Mo, Ga, Nb, Ta, or Mg, (b) adding a source of lithium, (c) treating the mixture obtained from step (b) thermally at at least two different temperatures: (c1) at 300 to 500° C. under an atmosphere that may comprise oxygen, (c2) at 500 to 600° C. under an atmosphere of oxygen, wherein the temperature in step (c2) is set to be higher than in step (c1).

Abstract: Process for making an electrode active material wherein said process comprises the following steps: (a) Providing a hydroxide TM(OH)2 or at least one oxide TMO or oxyhydroxide of TM or combination of at least two of the foregoing wherein TM contains at least 99 mol-% Ni and, optionally, in total up to 1 mol-% of at least one metal selected from Ti, Zr, V, Co, Zn, Ba, or Mg, (b) mixing said hydroxide TM(OH)2 or oxide TMO or oxyhydroxide of TM or combination with a source of lithium and an aqueous solution of a compound of Me wherein Me is selected from Al or Ga or a combination of the foregoing and wherein the molar amount of TM corresponds to the sum of Li and Me, (c) removing the water by evaporation, (d) treating the solid residue obtained from step (c) thermally at a temperature in the range of from 500 to 800° C. in the presence of oxygen.

Abstract: Described is a coated particulate material for use as electrode active material in an electrode and/or in a solid-state lithium-ion electrochemical cell and/or in an all solid-state lithium-ion electrochemical cell, comprising a plurality of core particles, each core particle comprising at least one nickel-containing complex layered oxide, and disposed on the surfaces of the core particles, a coating comprising carbonate ions, lithium and at least one further element. Further described is an electrode for use in a solid-state or all solid-state lithium-ion electrochemical cell and a respective electrochemical cell, each of them comprising said coated particulate material. Also described herein are methods of making the coated particulate material and the electrode, as well as respective uses of the coated particulate material.

Abstract: The present disclosure relates to a process for making a coated oxide material comprising: (a) providing a particulate material chosen from lithiated nickel-cobalt aluminum oxides and lithiated layered nickel-cobalt-manganese oxides wherein a nickel content ranges from 10 mole-% to 95 mole-% nickel, by total metal content in the particulate material, (b) optionally, treating the particulate material with an aqueous medium, followed by removing the aqueous medium, (c) treating the particulate material from step (a) or (b) with a metal amide or alkyl metal compound dissolved or slurried in an organic solvent, and (d) removing the organic solvent employed in step (c).

Abstract: A mesoporous, nanocrystalline, metal oxide construct particularly suited for capacitive energy storage that has an architecture with short diffusion path lengths and large surface areas and a method for production are provided. Energy density is substantially increased without compromising the capacitive charge storage kinetics and electrode demonstrates long term cycling stability. Charge storage devices with electrodes using the construct can use three different charge storage mechanisms immersed in an electrolyte: (1) cations can be stored in a thin double layer at the electrode/electrolyte interface (non-faradaic mechanism); (2) cations can interact with the bulk of an electroactive material which then undergoes a redox reaction or phase change, as in conventional batteries (faradaic mechanism); or (3) cations can electrochemically adsorb onto the surface of a material through charge transfer processes (faradaic mechanism).

Abstract: A mesoporous, nanocrystalline, metal oxide construct particularly suited for capacitive energy storage that has an architecture with short diffusion path lengths and large surface areas and a method for production are provided. Energy density is substantially increased without compromising the capacitive charge storage kinetics and electrode demonstrates long term cycling stability. Charge storage devices with electrodes using the construct can use three different charge storage mechanisms immersed in an electrolyte: (1) cations can be stored in a thin double layer at the electrode/electrolyte interface (non-faradaic mechanism); (2) cations can interact with the bulk of an electroactive material which then undergoes a redox reaction or phase change, as in conventional batteries (faradaic mechanism); or (3) cations can electrochemically adsorb onto the surface of a material through charge transfer processes (faradaic mechanism).

Abstract: A mesoporous, nanocrystalline, metal oxide construct particularly suited for capacitive energy storage that has an architecture with short diffusion path lengths and large surface areas and a method for production are provided. Energy density is substantially increased without compromising the capacitive charge storage kinetics and electrode demonstrates long term cycling stability. Charge storage devices with electrodes using the construct can use three different charge storage mechanisms immersed in an electrolyte: (1) cations can be stored in a thin double layer at the electrode/electrolyte interface (non-faradaic mechanism); (2) cations can interact with the bulk of an electroactive material which then undergoes a redox reaction or phase change, as in conventional batteries (faradaic mechanism); or (3) cations can electrochemically adsorb onto the surface of a material through charge transfer processes (faradaic mechanism).

Abstract: A mesoporous, nanocrystalline, metal oxide construct particularly suited for capacitive energy storage that has an architecture with short diffusion path lengths and large surface areas and a method for production are provided. Energy density is substantially increased without compromising the capacitive charge storage kinetics and electrode demonstrates long term cycling stability. Charge storage devices with electrodes using the construct can use three different charge storage mechanisms immersed in an electrolyte: (1) cations can be stored in a thin double layer at the electrode/electrolyte interface (non-faradaic mechanism); (2) cations can interact with the bulk of an electroactive material which then undergoes a redox reaction or phase change, as in conventional batteries (faradaic mechanism); or (3) cations can electrochemically adsorb onto the surface of a material through charge transfer processes (faradaic mechanism).

Abstract: A mesoporous, nanocrystalline, metal oxide construct particularly suited for capacitive energy storage that has an architecture with short diffusion path lengths and large surface areas and a method for production are provided. Energy density is substantially increased without compromising the capacitive charge storage kinetics and electrode demonstrates long term cycling stability. Charge storage devices with electrodes using the construct can use three different charge storage mechanisms immersed in an electrolyte: (1) cations can be stored in a thin double layer at the electrode/electrolyte interface (non-faradaic mechanism); (2) cations can interact with the bulk of an electroactive material which then undergoes a redox reaction or phase change, as in conventional batteries (faradaic mechanism); or (3) cations can electrochemically adsorb onto the surface of a material through charge transfer processes (faradaic mechanism).

Abstract: A mesoporous, nanocrystalline, metal oxide construct particularly suited for capacitive energy storage that has an architecture with short diffusion path lengths and large surface areas and a method for production are provided. Energy density is substantially increased without compromising the capacitive charge storage kinetics and electrode demonstrates long term cycling stability. Charge storage devices with electrodes using the construct can use three different charge storage mechanisms immersed in an electrolyte: (1) cations can be stored in a thin double layer at the electrode/electrolyte interface (non-faradaic mechanism); (2) cations can interact with the bulk of an electroactive material which then undergoes a redox reaction or phase change, as in conventional batteries (faradaic mechanism); or (3) cations can electrochemically adsorb onto the surface of a material through charge transfer processes (faradaic mechanism).

Abstract: A mesoporous, nanocrystalline, metal oxide construct particularly suited for capacitive energy storage that has an architecture with short diffusion path lengths and large surface areas and a method for production are provided. Energy density is substantially increased without compromising the capacitive charge storage kinetics and electrode demonstrates long term cycling stability. Charge storage devices with electrodes using the construct can use three different charge storage mechanisms immersed in an electrolyte: (1) cations can be stored in a thin double layer at the electrode/electrolyte interface (non-faradaic mechanism); (2) cations can interact with the bulk of an electroactive material which then undergoes a redox reaction or phase change, as in conventional batteries (faradaic mechanism); or (3) cations can electrochemically adsorb onto the surface of a material through charge transfer processes (faradaic mechanism).

Abstract: A mesoporous, nanocrystalline, metal oxide construct particularly suited for capacitive energy storage that has an architecture with short diffusion path lengths and large surface areas and a method for production are provided. Energy density is substantially increased without compromising the capacitive charge storage kinetics and electrode demonstrates long term cycling stability. Charge storage devices with electrodes using the construct can use three different charge storage mechanisms immersed in an electrolyte: (1) cations can be stored in a thin double layer at the electrode/electrolyte interface (non-faradaic mechanism); (2) cations can interact with the bulk of an electroactive material which then undergoes a redox reaction or phase change, as in conventional batteries (faradaic mechanism); or (3) cations can electrochemically adsorb onto the surface of a material through charge transfer processes (faradaic mechanism).

Abstract: The current invention relates to a method of making metal oxide nanoparticles comprising the reaction of—at least one metal oxide precursor (P) containing at least one metal (M) with—at least one monofunctional alcohol (A) wherein the hydroxy group is bound to a secondary, tertiary or alpha-unsaturated carbon atom—in the presence of at least one aliphatic compound (F) according to the formula Y1—R1—X—R2—Y2, wherein—R1 and R2 each are the same or different and independently selected from aliphatic groups with from 1 to 20 carbon atoms, —Y1 and Y2 each are the same or different and independently selected from OH, NH2 and SH, and —X is selected from the group consisting of chemical bond, —O—, —S—, —NR3—, and CR4R5, wherein R3, R4 and R5 each are the same or different and represent a hydrogen atom or an aliphatic group with from 1 to 20 carbon atoms which optionally carries functional groups selected from OH, NH2 and SH.